Distribution of acquired antibiotic resistance genes among Enterococcus spp. isolated from a hospital in Baotou, China

Objective This study investigated the distribution of acquired antibiotic resistance genes in Enterococcus species isolated from clinical patients in Baotou, China. Result A total of 73 enterococca lisolates from clinical samples were collected from December 2016 to September 2017. Of the 73 enterococcal isolates, 36 (49.3%), 35 (47.9%), 1 (1.4%), and 1 (1.4%) were identified as E. faecium, E. faecalis, E. gallinarum, and E. raffinosus, respectively. The resistance rates of the enterococci to nitrofurantoin, tetracycline, gentamicin (high-level), ampicillin, ciprofloxacin and erythromycin were 24.7%, 49.3%, 50.7%, 54.8%, 74.0% and 89.0%, respectively. The most prevalent aminoglycoside resistance genes were aac(6′)-Ie-aph(2″)-Ia (64.9%) and aph(3′)IIIa (64.9%). The most common erythromycin ribosome methylation gene was erm(B) (67.7%), followed by erm(A) (4.6%) and erm(C) (1.5%). The tetracycline resistance gene tetM was found to be present in 100.0% of the tetracycline-resistant strains of enterococci. Thus, E. faecium and E. faecalis were identified as the species of greatest clinical importance associated with hospital-acquired enterococcal infections in Baotou, China. The antimicrobial resistance genes aac(6′)-Ie-aph(2″)-Ia, aph(3′)IIIa, tetM, and erm(B) were significantly more prevalent among the enterococcal isolates. Therefore, action should be taken to monitor drug resistance and antimicrobial resistance genes to manage multi-drug-resistant enterococcal infections. Electronic supplementary material The online version of this article (10.1186/s13104-019-4064-z) contains supplementary material, which is available to authorized users.


Introduction
Enterococci have long been considered symbiotic organisms of humans that have the potential to accidentally invade the host [1]. Recently, Enterococcus species have emerged as important pathogens causing hospitalacquired and community-acquired abdominal infections [2]. The common infection sites are the urinary tract, surgical sites, respiratory tract, gastrointestinal tract, skin and soft tissue. In addition, the incidence of infections caused by multi-drug-resistant isolates of enterococci is increasing worldwide, which is a serious problem for clinical anti-infective therapy [3].
Many studies have reported that enterococci are resistant to a wide range of antimicrobial agents via intrinsic and acquired mechanisms [4]. The mechanism underlying the acquisition of antibiotic resistance genes has been recognized for several decades. High-level aminoglycoside resistance is primarily due to the acquisition of genes encoding aminoglycoside-modifying enzymes (AMEs), such as aac(6′)-Ie-aph(2″)-Ia, aph(2″)-Ib, aph(2″)-Ic, aph(2″)-Id, and aph(3′)IIIa [5]. Erythromycin resistance among enterococci is associated with the presence of erythromycin resistance methylase (erm) genes, such as erm(A), erm(B), and erm(C). The predominant erm gene in erythromycin-resistant isolates of enterococci is the erm(B) gene, which encodes the ribosomal RNA methylase [6]. Moreover, there are currently over 40 different acquired tetracycline resistance genes recognized. The tet(M) gene is the tetracycline resistance gene with the broadest host range [7]. The protein encoded by the tetM gene blocks the binding of tetracycline to the ribosome by combining with the 50S ribosomal subunit, causing a conformational change in the ribosome that subsequently produces drug resistance.
The difficulty in treating enterococcal infections is associated with antimicrobial resistance. Therefore, the study of the distribution of resistance genes and resistance mechanisms of enterococci to guide clinical treatment is particularly important. The aim of the present study was to determine the antibiotic susceptibility of enterococci, examine the presence of genes encoding AMEs (including aac(6′)-Ie-aph(2″)-Ia, aph(2″)-Ib, aph(2″)-Ic, aph(2″)-Id, and aph(3′)-IIIa) and the erm factors (including erm(A), erm(B), and erm(C)), and identify the tet(M) gene of enterococcal isolates from clinical patients in Baotou, China.

Bacterial strains and identification
A total of 73 clinical isolates of enterococci were collected from the Second Affiliated Hospital of Baotou Medical College in Baotou, China, between December 2016 and September 2017. Duplicate and contaminated isolates were excluded from the study. Institutional ethical clearance was obtained. Conventional biochemical tests and the Phoenix100 automatic system (BD, USA) were used to identify the isolates as enterococci. Identifications of E. faecalis, E. faecium and the other strains were further confirmed via PCR analysis as described previously [8].

Amplification of antimicrobial resistance genes
Total DNA was extracted from enterococci according to the instruction manuals of commercial DNA extraction kits (Tiangen Biotech Co., Ltd., Beijing, China). The presence of the antimicrobial resistance genes was detected by PCR (see Additional file 1: Table S1) [10][11][12][13]. PCR amplification was performed using 5 μl of template DNA, 2 μl of each primer (100 pmol), and 25 μl of 2 × Taq PCR MasterMix (Solarbio Science & Technology Co., Ltd., Beijing, China) in a total reaction volume of 50 μl. The PCR conditions consisted of an initial denaturation step at 94 °C for 3 min, followed by 35 cycles of denaturation at 94 °C for 30 s, annealing for 30 s, and elongation at 72 °C for 1 min. A final extension step was carried out at 72 °C for 5 min.

Statistical analysis
All statistical analyses were performed using Statistical Package for Social Sciences (SPSS) software (version 17.0). Probability values (p) of < 0.05 were considered statistically significant.

Discussion
It has been shown that enterococci are opportunistic nosocomial pathogens capable of causing various infectious diseases. Many Enterococcus species have been reported, and E. faecium and E. faecalis are the most common human infectious strains of Enterococcus [14,15]. This finding is similar to that observed in the present report.
It appears that the increased prevalence of multi-drugresistant Enterococcus species has become a major public health problem. In the current study, a high percentage of enterococci exhibited resistance to erythromycin (89.0%), ciprofloxacin (74.0%), ampicillin (54.8%), gentamicin (high-level) (50.7%), tetracycline (49.3%) and nitrofurantoin (24.7%). However, the isolates were highly sensitive to the following antibiotics: teicoplanin (0 resistant strains), linezolid (0 resistant strains), and vancomycin (0 resistant strains), similar to other reports [16]. In this study, the rate of ampicillin resistance in E. faecium species showed a significant difference when compared to that of E. faecalis, which is in agreement with previous studies [17].
The presence of AME genes, such as aac(6′)-Ie-aph(2″)-Ia, aph(2″)-Ib, aph(2″)-Ic, aph(2″)-Id, and aph(3′)IIIa, that are responsible for high-level gentamicin resistance,   have been extensively reported [18]. Our previous studies found that aac(6′)-Ie-aph(2″)-Ia was the most common AME gene [15]. In the current study, a high prevalence of the aph(3′)-IIIa gene was also found. We further showed that 37.8% of the HLGR enterococcal isolates carried both aac(6′)-Ie-aph(2″)-Ia and aph(3′)-IIIa, which was higher than our previous results [15]. Moreover, 8.1% of the HLGR enterococcal isolates did not carry any of the examined AME genes. This was lower than that previously reported by Li et al. [19]. The presence of a wide range of erythromycin resistance genes in Enterococcus species has been reported elsewhere [20]. In the present study, the most abundant erm gene was erm(B), followed by erm(A) and erm(C). A Previous study by Quiñones Pérez et al. found that 70.9% of erythromycin-resistant enterococcal isolates examined in their study carried erm(B) [21]. This value is close to that obtained in our present study (67.7%). In addition, the erm(A) and erm(C) genes were only detected in erythromycin-resistant isolates of E. faecium, which was a rarer occurrence than that previously reported [22]. Moreover, 17 isolates (26.2%) of the erythromycin-resistantent erococci were negative for the erm genes examined in this study. It is possible that other genes could be associated with erythromycin-resistant enterococcal isolates, such as erm(D), erm(E), erm(F), erm(G), erm(Q), and the macrolide efflux pump (msrA).
Acquired resistance to tetracyclines in enterococci is often by mobile genetic elements [23]. The detection of the tetM gene by PCR has frequently been used to monitor tetracycline resistance in microbial populations [24]. The results of this study showed that 100% of the tetracycline-resistant Enterococcus isolates carried the tetM gene, which was higher than previously reported prevalences [25].

Conclusions
Enterococcus species have become a significant cause of hospital-acquired infections. The present study showed that enterococci recovered from clinical samples in Baotou, China, contained a variety of antimicrobial resistance genes. These results will be helpful in clarifying the transmission mechanisms of antibiotic-resistant Enterococcus species.

Limitations
This study tried to address the distribution of acquired antibiotic resistance genes among Enterococcus species isolated from a hospital in Baotou, China. However, the study was not without limitations. This was a small study that could not include additional samples of Enterococcus species taken from this region. In addition, the study utilized PCR-based methods to detect some common acquired antibiotic resistance genes, and tests for several additional antibiotic resistance genes will be needed.

Additional files
Additional file 1: Table S1. PCR primers used in the amplification of resistance genes.
Additional file 2: Table S2. The resistance rate of the clinical isolates of enterococci species to various antimicrobial agents.
Additional file 3: Table S3. Differences in the prevalence of resistance genes between E. faecalis and E. faecium were compared using the Chi square test, with a p value < 0.05 indicating statistical significance.

Authors' contributions
YT conducted the study, collected the data, performed the analysis of the data, and prepared the manuscript; HY conducted the study, collected the data, and performed the analysis of the data; ZW designed and supported the study, and edited the manuscript. All authors read and approved the final manuscript.